Solid phase peptide synthesis via side chain attachment

ABSTRACT

The present application discloses peptides and peptaibols of high purity may be obtained by solid phase peptide synthesis using as the starting resin hydroxy amino acids, hydroxy amino acid amides, hydroxy amino alcohols or small peptides containing hydroxy amino acids attached to polymers through their side chain.

REFERENCE TO SEQUENCE LISTING SUBMITTED VIA EFS-WEB

This application includes a sequence listing in .txt format that iselectronically submitted via EFS-Web. The .txt file contains a sequencelisting entitled “2013-05-13 543809 (DYT-006)_ST25.txt” created on May13, 2013 and is 9,292 bytes in size. The sequence listing contained inthis .txt file is part of the specification and is hereby incorporatedby reference herein in its entirety.

SUMMARY

Peptides and peptaibols of high purity were obtained by solid phasepeptide synthesis using as the starting resin hydroxy amino acids,hydroxy amino acid amides, hydroxy amino alcohols or small peptidescontaining hydroxy amino acids attached to polymers through their sidechain.

DEFINITIONS AND ABBREVIATIONS

“Hya” or “hydroxyl amino acid(s)” means amino acids that contain ahydroxyl (—OH) group.

N-terminus or amino terminus is the first amino acid in a peptide chain.

C-terminus or carboxy terminus is the last amino acid in the peptidechain as shown below.

“P” or “solid support” or “resin” means an insoluble material containinga functional group(s) suitable to react and link with an amino acid orpeptide. The solid support or resins are well known in the art.

“Alkyl” such as C₁₋₁₀alkyl or C₁₋₆alkyl, means a branched or unbranchedfully saturated acyclic aliphatic hydrocarbon group (i.e. composed ofcarbon and hydrogen containing no double or triple bonds). In someembodiments, alkyls may be substituted or unsubstituted. Alkyls mayinclude, but are not limited to methyl, ethyl, propyl, isopropyl, butyl,isobutyl, tert-butyl, pentyl, hexyl, and the like, and in someembodiment, each of which may be optionally substituted. Non-exclusivealkyl substituents may include C₁₋₃alkoxy, halo (F, Cl, Br or I), nitro,amino, —SH and —OH.

“Attachment” means the linking of an amino acid or a peptide or peptidederivative to an insoluble support.

“Hse” means homoserine; “Hnv” means hydroxylnorvaline.

“SPPS” or “solid phase peptide synthesis” means the synthesis of apeptide with the use of a resin as described herein.

“pNA” means 4-nitro anilide.

“DME” means dimethoxy ethane.

“Acid sensitive resin” means an insoluble material or resin containing afunctional group(s) suitable to react and link with an amino acid orpeptide, which may be cleaved from the peptide by acidic treatment.

“Acid sensitive protecting group” means a protecting group which may becleaved from the amino acid or peptide or peptide derivative by acidictreatment or under acidic condition.

“Peptaibol” means a peptide which contain at its C-terminal position anamino alcohol instead of an amino acid or an amino acid amide.

“Step-by-step” means the method of peptide synthesis where any of theamino acids contained in the peptide chain is introduced individuallyand sequentially. The method may or may not involve an intermediatepurification step.

“Protected peptide” means the peptide with all functional groups blockedor protected by protecting groups.

“Partially protected peptide” means the peptide which contains at leastone functional group blocked or protected by a protecting group.

Solid phase peptide synthesis is traditionally performed by theattachment of the C-terminal amino acid through its α-carboxyl functionon a suitable solid support and elongating the peptide chain towards theamino terminal of the peptide by adding sequentially the amino acidresidues in the gradually growing peptide chain. Several hundredthousands of publications and patents describe this methodology and itsapplication for the production of peptide pharmaceuticals.

In contrary to the attachment of the C-terminal carboxyl function,attachment of amino acids and peptides through an amino acid side chainon suitable resins and their application in SPPS is described verybriefly, in particular in less than 30 publication and patents. Most ofthese publications describe the attachment of the amino acids through aside chain carboxyl function of Asp and Glu. To our knowledge, thereports of the side chain attachment of amino acids through a side chainhydroxyl function and application in peptide synthesis are limited: Theside chain attachment of Fmoc-Hya-pNA (Formula A1) [A. Bernhardt, M.Drewello and M. Schutkowski, The solid-phase synthesis ofside-chain-phosphorylated peptide-4-nitroanilides J. Peptide Res. 50,1997. 143-152] and their use for the synthesis of short nitroanilidesubstrates, the synthesis of Fmoc-Hya-Oallyl esters (Formula A2 [L.Rizzi, K. Cendic, N. Vaiana, S. Romeo, Alcohols immobilization onto2-chlorotritylchloride resin under microwave irradiation, TetrahedronLetters 52 (2011) 2808-2811]) on 2-chlorotrityl resin with the aid ofmicrowaves for application in the preparation of cyclic peptides and thesynthesis of Fmoc-Tyr-O-methyl ester (Formula A3 [C. Cabrele, M. Langerand A. G. Beck-Sickinger, Amino Acid Side Chain Attachment Approach andIts Application to the Synthesis of Tyrosine-Containing Cyclic Peptides,J. Org. Chem. 1999, 64, 4353-4361]), attached on resins of thebenzyl-type by the Mitsunobu redox-alkylation of the Tyr-phenoxyfunction and their application for the synthesis of short cyclicpeptides. To our knowledge, the side chain attachment of Hse and Hyphave never been disclosed. In addition, the application of side chainattached Hya on acid sensitive resins for the solid phase synthesis ofprotected peptides, protected peptide fragments and of protected peptideamides and peptaibols have not been reported.

Solid Phase Peptide Synthesis

In one embodiment, there is provided an improved synthesis of peptideacids, peptide amides, and peptaibols of pharmaceutical interest.

In one aspect of the present application, the peptides were producedvery efficiently in high yield and purity by attaching a hydroxy aminoacid through its amino acid side chain, or a small peptide which containin its sequence a hydroxy amino acid on a resin of the trityl orbenzhydryl-type, resulting in amino acid-resin conjugates or peptideresin conjugates of Formula I-IV, wherein P is a solid-phase supportselected from the supports used in solid phase peptide synthesis, Pr¹ isH or an amino protecting group selected from Fmoc, Boc, Trt, Dde andAlloc, wherein Pr² is an acid sensitive hydroxyl protecting groupselected from Trt, Clt, Mmt, Mtt, Dpm and tBu, wherein Hya is a hydroxyamino acid selected from D- or L-Ser, Thr, Tyr, Hse, Hyp, Hnv etc., andA is OH, an acid sensitive alkoxy group selected from OTrt, OClt, OMmt,OMtt, ODpm and OtBu, NH₂, NHR¹, NR¹R² wherein R¹ and R² areindependently an alkyl group a protected or semi protected peptidecontaining 1-10 amino acids in its sequence.

In another embodiment, we disclose that peptaibols, such as octreotide,were obtained by solid phase synthesis using the resin-bound aminoalcohols of the Formula III-VI selected from amino alcohols which arederived from the naturally occurring hydroxy amino acids, wherein P, X,V, Z and Pr¹ are as defined above, wherein R³, R⁴ are alkyl, aryl oraralkyl groups, and Pr² is an acid sensitive protecting group of thetrityl, benzhydryl or benzyl type.

In addition we disclose for the first time that peptides prepared withthe application of resins of the Formula I-IV, where the peptides areattached through the side chain hydroxyl function of a hydroxyamino acidon resins of the trityl type, may be cleaved from the resin by mildacidic treatment and wherein the side chain protecting groups of the tBuand benzyl-type remain intact. In one aspect, the cleavage from theresin occurs by the treatment with 1-3% acid solutions, such as TFA,diluted HCl solutions, optionally adding scavengers, in a solvent. Inanother aspect, the cleavage may be performed in a solvent such as DCMor acetone. Such partially protected peptides have been found to beuseful in the synthesis of longer peptides by fragment condensation insolution or on solid phase. The present method expands the versatilityof the application of the resins described herein, and also results insignificantly improving the purity of the resulting pharmaceuticalpeptides, and at the same time, substantially reducing the cost of theirsynthesis.

Several peptides of pharmaceutical interest were produced asrepresentative of the new process described herein, either by thestep-by-step procedure or by fragment condensation in solution and onsolid phase; or a combination thereof. The examples below arerepresentative and do not limit their application in any way to otherpeptides.

Lanreotide:

In one embodiment, Lanreotide was produced by solid phase synthesisusing resin-bound Thr-amide as shown below:

Human Insulin B-Chain:

Optionally the human insulin B chain was synthesized by SPPS. In oneaspect, the synthesis begins from the resin-bound Thr-t-butyl ester asdescribed in the example, using the 4-methoxy benzhydryl resin.Optionally the synthesis may also be performed on solid phase bycondensing the 1-8 partially protectedBoc-Phe-Val-Asn(Trt)-Gln(Trt)-His(Trt)-Leu-Cys(Trt)-Gly-OH fragment withthe resin-bound 9-30 fragment; or after the selective cleavage of thepartially protected 9-30 fragment from the resin with condensation insolution of the 1-8 and 9-30 fragments.

Salmon Calcitonin:

Optionally salmon calcitonin may be produced starting the synthesis fromresin bound Fmoc-Thr-Pro-NH₂. The peptide chain is then elongated usingFmoc-amino acids.

Optionally the resin-bound salmon calcitonin is produced by fragmentcondensation on the resin as shown above, for example, or in solution asshown below using 2-4 fragments.

Octreotide:

In another embodiment, octreotide was efficiently synthesized by theattachment of Fmoc-threoninol-OTrt to the 4-methoxybenzhydryl resinthrough the side chain of threoninol as shown below, followed by theoctreotide chain assembly using Fmoc-amino acids and finally cleavingoctreotide from the resin with subsequent or simultaneous Cys-oxidation.Fmoc-threoninol-OTrt is much easier to be produced than theFmoc-Thr(tBu)-ol which may be attached onto the resin through thehydroxymethyl group of threoninol on a suitable resin. This is becauseH-Thr(OtBu)-ol, used as the starting material for the production ofFmoc-Thr(tBu)-ol, is much more difficult to be produced thanFmoc-threoninol-OTrt used in the attachment of threoninol through itsside chain onto the resin.

Exenatide:

In another example, Fmoc-Ser-NH₂ was attached through its side chain ontrityl resin and used for the synthesis of exenatide. The synthesis maybe performed by the step-by-step manner or by fragment condensation insolution after cleavage a partially protected exenatide fragment fromthe resin by mild acidic treatment or on solid phase, as describedbelow. According to this method, most impurities typically formed duringthe synthesis of many Pro and Gly residues containing peptides arecompletely avoided and peptides of high purity are obtained. The methodalso allows the complete avoidance of impurities originating from thecleavage of peptides from peptide amide linkers using other methodsknown in the art, which significantly reduce the yields and purity ofthe peptide.

In one aspect, exenatide may be produced by cleavage of the partiallyprotected peptide 12-39 from the resin and condensing it in solution asshown below with the partially protected 1-11 fragment. Alternatively,the condensation to obtain protected exenatide may be performed with thefragments 1-13 and 14-39.

Pramlintide:

The method is also highly effective in the production of amylinpeptides. In one aspect, the side chain attachment may be performedusing one of the C-terminal Ser, Thr or Tyr residues of amylin or itsderivatives such as pramlintide. The synthesis may be performed in thestep-by-step manner or by fragment condensation in solution or on solidphase. By incorporating pseudoprolines (Ψ, see Mutter et al, PeptideRes. (1995 8, 145) into the growing peptide chain, the synthesis isaccelerated and the purity of the peptide obtained is improved.

Alternatively, the synthesis of pramlintide may be performed in liquidphase with equal success concerning the purity and the yield of theobtained pramlintide. In one embodiment, the protected peptide which isbound on the resin through the side chain of Fmoc-Tyr-NH₂ may bequantitatively cleaved from the resin with the side chain protectinggroups of the tBu-type remaining intact, using mild acidic treatment atvarious positions of the peptide chain. In one example, as shown belowthe partially protected 1-10 fragment prepared on the 2-chlorotritylresin in the step by step manner was condensed successfully with thepartially protected 11-37 fragment amide.

Pramlintide:

Tetracosactide (ACTH 1-24):

In another example, ACTH 1-24 was effectively prepared starting fromresin-bound Fmoc-Tyr-Pro-OtBu by the step by step procedure or bycondensing the 1-10 partially protected fragment in solution with the11-24 fragment or with the resin-bound 11-24 fragment, as shown below.

Bivalirudin:

In another example, bivalirudin was produced in high yield and highpurity starting from resin-bound Fmoc-Tyr-Leu-OtBu, extending thepeptide chain in the step-by-step manner with Fmoc-amino acids andfinally deprotecting and cleaving the peptide from the resin as shownbelow.

Alternatively, bivalirudin was obtained by the condensation of protectedfragments on the resin or by cleaving a partially protected peptidewhich contain 4-15 amino acid residues from the resin and condensing itin solution with a bivalirudin fragment which contain 5-16 amino acids.The bivalirudin synthesis by fragment condensation on the resin of the1-10 partially protected bivalirudin fragment with the resin-bound 11-20partially protected bivalirudin fragment is described below.

EXAMPLES Example 1 Preparation of Fmoc-Thr(4-methoxybenzhydrylpolystyryl)-OtBu

30 mmol Fmoc-Thr-OtBu prepared from H-Thr-OtBu by its reaction withFmoc-OSu following conventional methods were reacted with 20 g (30 mmol)of 4-methoxybenzhydryl polystyrene resin (product of CBL-Patras) and 60mmol DIPEA in 250 ml THF for 10 h at RT. To the mixture were then added60 mmol methanol and the mixture was shaken for additional 4 h. Theresin was filtered and washed 3× with THF/MeOH/DIPEA (85:10:5), 6×DMF,4×IPA, 3×DEE and dried in vacuum to constant weight. 29 g of resin-boundFmoc-Thr-OtBu were obtained with a loading of 0.95 mmol/g resin.

Example 2 Fmoc-Thr(4-methoxybenzhydryl polystyryl)-O-Clt

30 mmol Trt-Thr-OMe prepared from H-Thr-OMe by its reaction withTrt-Cl/Me₃SiCl and DIPEA following conventional methods were reactedwith 20 g (30 mmol) of 4-methoxy 4′-polystyryl benzhydryl bromide resin(product of CBL-Patras) and 60 mmol DIPEA in 250 ml THF for 10 h at RT.To the mixture were then added 60 mmol methanol and the mixture wasshaken for additional 4 h. The resin was filtered and washed 3× withTHF/MeOH/DIPEA (85:10:5), 3×DCM, 3×1% TFA in DCM, 4×THF, 3× 1N—LiOH inTHF/Water/Methanol (70:15:15), 3×THF/Water (75:25) 4×DMF and thenreacted for 2 h at RT with 60 mmol Fmoc-OSu and 30 mmol DIPEA, washed3×DMF, 3×DCM and then reacted for 3 h at RT with 50 mmol Trt-Cl and 50mmol DIPEA, washed 4×DMF, 6×DEE and dried in vacuum to constant weight.32.3 g of resin-bound Fmoc-Thr-OtBu were obtained with a loading of 0.78mmol/g resin.

Example 3 Fmoc-Throl(4-methoxy benzhydryl polystyryl)-O-Clt

A) Starting from Fmoc-threoninol

50 mmol commercial Fmoc-threoninol (CBL-Patras) in 350 ml DCM werereacted with 55 mmol monomeric Clt-Cl and 55 mmol DIPEA for 4 h at RT.The obtained mixture was extracted as usual with water and the DCM phasewas dried over anhydrous sodium sulphate and filtered. To the resultingsolution 30 g of 4-methoxy, 4-polystyryl benzhydryl bromide (CBL-Patras)were added and 50 mmol DIPEA and the resulting mixture was stirred for 4h at RT. The resin was filtered and washed 6×DMF, 4×IPA and 4×DEE anddried in vacuum to constant weight. 38.4 g of resin-boundFmoc-threoninol were obtained with a loading of 0.82 mmol/g.

B) Starting from Trt-Thr(Resin)-OMe

30 mmol Trt-Thr-OMe prepared from H-Thr-OMe by its reaction withTrt-Cl/Me₃SiCl and DIPEA following conventional methods were reactedwith 20 g (30 mmol) of 4-methoxy 4′-polystyryl benzhydryl bromide resin(product of CBL-Patras) and 60 mmol DIPEA in 250 ml THF for 10 h at RT.To the mixture were then added 60 mmol methanol and the mixture wasshaken for additional 4 h. The resin was filtered and washed 3× withTHF/MeOH/DIPEA (85:10:5), 5×THF, and then reacted with 30 mmol LiBH₄ inTHF. The resin was then filtered and washed 6×THF, 4×DCM, 6× 1% TFA inDCM, 3× with DMF/DIPEA (97:3) and then reacted for 2 h at RT with 60mmol Fmoc-OSu and 30 mmol DIPEA, washed 3×DMF, 3× DCM and then reactedfor 3 h at RT with 50 mmol Clt-Cl and 50 mmol DIPEA, washed 4× DMF,6×IPA and 6×DEE and dried in vacuum to constant weight. 34.7 g ofresin-bound Fmoc-Throl-O-Clt were obtained with a loading of 0.74 mmol/gresin.

Example 4 Fmoc-Ser(trityl resin)-NH₂

50 mmols of Fmoc-Ser-NH₂, prepared according to standard proceduresknown in the art, were dissolved in 0.5 liter of DCM. To the suspension30 g of Trityl chloride resin (36 mmol) were added and 65 mmol DIPEA andthe mixture was stirred for 6 h at RT. Then and then 25 ml methanol and30 mmol DIPEA were added and the mixture was stirred for additional 2 hat RT. The resin was then filtered and washed 3× with DCM/MeOH/DIPEA(90:5:5), 5×DMF, 4× IPA, 4×DEE and dried in vacuum to constant weight.41.1 g of Fmoc-Ser-NH₂-containing resin were obtained with a loading of0.71 mmol/g.

Example 5 Fmoc-Tyr(2-chlorotrityl resin)-NH₂

Following the above procedure, 50 mmol Fmoc-Tyr-NH₂ and 30 g 2-CTCchloride resin gave 43.7 g resin with a loading of 0.81 g Tyr/g resin.

Example 6 Fmoc-Hyp(4-methyl benzhydryl resin)-NH₂

Following the above procedure 50 mmol Fmoc-Hyp-NH₂ and 30 g 4-methylbenzhydryl bromide resin gave 39.8 g resin with a loading of 0.49 gHyp/g resin.

Example 7 Fmoc-Thr(4-methoxybenzhydryl resin)-Pro-NH₂

50 mmols of Fmoc-Thr-Pro-NH₂ prepared from coupling of Fmoc-Thr(tBu)-OHwith H-Pro-NH₂ according to standard procedures known in the art, weredissolved in 0.5 liter of DME. To the resulting solution 30 g of4-methoxy benzhydryl bromide resin (45 mmol) were added and 65 mmolDIPEA and the mixture was stirred for 6 h at RT. Then 25 ml methanol and50 mmol DIPEA were added and the mixture was stirred for additional 2 hat RT. The resin was then filtered and washed 3× with DME/MeOH/DIPEA(90:5:5), 5×DMF, 4×IPA, 4×DEE and dried in vacuum to constant weight.44.5 g of Fmoc-Thr-Pro-NH₂ containing resin with a loading of 0.77mmol/g was obtained.

Example 8 Fmoc-Tyr(2-chlorotrityl resin)-Pro-OtBu

50 mmols of Fmoc-Tyr-Pro-OtBu were prepared according to standardprocedures known in the art, were dissolved in 0.5 liter of DCM. To theresulting solution 30 g of 2-chlorotrityl chloride resin (48 mmol) wereadded and 65 mmol DIPEA and the mixture was stirred for 12 h at RT. Then25 ml methanol and 50 mmol DIPEA were added and the mixture was stirredfor additional 2 h at RT. The resin was then filtered and washed 3× withDCM/MeOH/DIPEA (90:5:5), 5×DMF, 4×IPA, 4×DEE and dried in vacuum toconstant weight. 44.5 g of Fmoc-Tyr-Pro-OtBu containing resin with aloading of 0.64 mmol/g was obtained.

Example 9 Fmoc-Tyr(2-chlorotrityl resin)-Leu-OtBu

50 mmols of Fmoc-Tyr-Leu-OtBu, prepared according to standard proceduresknown in the art, were dissolved in 0.5 liter of THF. To the resultingsolution 30 g of 2-CTC chloride resin (48 mmol) were added and 65 mmolDIPEA and the mixture was stirred for 12 h at 60° C. Then 25 ml methanoland 50 mmol DIPEA were added and the mixture was stirred for additional2 h at RT. The resin was then filtered and washed 3× with DCM/MeOH/DIPEA(90:5:5), 5×DMF, 4×IPA, 4×DEE and dried in vacuum to constant weight.44.5 g of Fmoc-Tyr-Leu-OtBu-containing resin with a loading of 0.64mmol/g was obtained.

Example 10 Solid-Phase Synthesis of Peptides and Protected PeptideSegments

General Procedure.

A1. Preparation of loaded 2-chlorotrityl resins, general procedure

2-Chlorotrityl chloride resin (CTC-Cl) (100 g; loading 1.6 mmol/g) ofCBL-Patras, is placed in a 2 L peptide synthesis reactor and is swollenwith 700 mL dichloromethane (DCM):dimethylformamide (DMF) 1:1 for 30 minat 25° C. The resin is filtered and a solution of 100 mmol Fmoc-aminoacid and 300 mmol diisopropylethylamine (DIEA) in 500 mL DCM is added.The mixture is stirred under nitrogen for 2 hours at 25° C. Then, theremaining active sites of the 2-CTC resin are neutralised by adding 10mL of methanol (MeOH) and reacting for 1 hour. The resin is filtered andwashed twice with 400 mL DMF. The resin is filtered and treated twicewith 500 mL 25% by volume of piperidine in DMF for 30 min. The resin isthen washed four times with 500 mL DMF. The resin is deswelled with 3washes with 500 mL of isopropanol (IPA). The resin is dried to constantweight. On the resin was bound the 70-95% of the mmol of the used aminoacid.

B. Solid-Phase Synthesis, a General Protocol

The solid-phase synthesis was performed at 24° C. with 1.0 g amino acidor peptide esterified to the resin of the trityl or benzhydryl type orattached through its side chain as described in Part A or in theexamples Example 1. The following protocol was used in the synthesis.

B1. Swelling of the Resin

The resin was placed in a 15 ml reactor and treated twice with 7 mL NMP,followed by filtration.

B2. Activation of the Amino Acid

The amino acid (3.0 equiv.) and 1-hydroxybenzotriazole (4.0 equiv.) wasweighted and dissolved in a reactor with 2.5 their volume in NMP andcooled to 0° C. DIC was then added (3.0 equiv.) and the mixture wasstirred for 15 min.

B3. Coupling

The solution which was prepared in B2 was then added to the B1 reactor.The reactor was washed once with one volume of DCM and was added to thereactor which was stirred for 1-3 h at 25°-30° C. In a sample the KaiserTest was performed to determine the completion of the reaction. If thecoupling reaction was not completed after 3 h (positive Kaiser Test),the reaction mixture was filtered and recoupled with a fresh solution ofactivated amino acid. After completion of the coupling the reactionmixture was filtered and washed 4 times with NMP (5 volumes per wash).

B4. Removal of the Fmoc-Group

The resulting resin in B3 was filtered and then treated for 30 min with5 mL of a solution which contained 25% by volume of piperidine. Theresin is then washed three times with 5 mL NMP.

B5. Elongation of the Peptide Chain

After the incorporation of each amino acid the steps B1-B5 were repeateduntil the completion of the peptide chain.

For the introduction of each individual amino acid the followingFmoc-amino acids were used: Fmoc-Ala-OH, Fmoc-Arg(Pbf)-OH, Fmoc-Asn-OH,Fmoc-Asn(Trt)-OH, Fmoc-D-Cys(Trt)-OH, Fmoc-Cys(Trt)-OH, Fmoc-Gln-OH,Fmoc-Gln(Trt)-OH, Fmoc-Glu(tBu)-OH, Fmoc-Gly-OH, Fmoc-His(Trt)-OH,Fmoc-Hyp(tBu)-OH, Fmoc-Ile-OH, Fmoc-Leu-OH, Fmoc-Met-OH, Fmoc-D-Phe-OH,Fmoc-Phe-OH, Fmoc-Pro-OH, Fmoc-Ser(tBu)-OH, Fmoc-Ser(Trt)-OH,Fmoc-Thr(tBu)-OH, Fmoc-Ser(Trt)-OH, Fmoc-D-Trp-OH, Fmoc-Trp-OH,Fmoc-D-Trp(Boc)-OH, Fmoc-Trp(Boc)-OH, Fmoc-Tyr(tBu)-OH,Fmoc-Tyr(Clt)-OH, Fmoc-Val-OH, Boc-D-Cys(Trt)-OH, Boc-His(Trt)-OH,Boc-Lys(Boc)-OH, Boc-D-2-Nal-OH, Boc-D-Phe-OH, Boc-Ser(tBu)-OH.

C. General Method for the Acidic Cleavage from the CTC-Resin of Peptidesand of Protected Peptide Segments, which Contain Fmoc- or Boc-Groups ontheir N-terminus.

The resin-bound peptide or peptide segment which was produced asdescribed above in B1-B5 was washed 4 times with 5 mL NMP, 3 times with5 ml IPA and finally 5 times with 7 ml DCM to remove completely anyresidual NMP or other basic components. The resin was then cooled to 0°C., filtered from DCM and was treated twice with a solution of 10 mL1-2% TFA/DCM at 5° C. The mixture is then stirred 20 min at 0° C. andfiltered. The resin is then washed three times with 10 mL DCM. Pyridineis then added to the filtrates (1.3 equiv. relative to TFA) toneutralize the TFA. The cleavage solution in DCM is then mixed with anequal volume of water. The resulting mixture is distilled at reducedpressure to remove DCM (350 torr at 28° C.). The peptide or peptidesegment precipitated after the removal of DCM. The resulting peptide iswashed then with water and dried at 30-35° C. under 15 Torr vacuum.

Example 11 Synthesis of Resin-Bound Protected Peptides by theCondensation of an N-Terminal Protected Fragment with a Resin-BoundC-Terminal Protected Fragment

General Procedure

To a solution of 0.15 mmol/ml of an N-terminal protected peptidefragment in DMSO/DCM (95:5) are added 0.2 mmol HOBt and the resultingsolution is cooled to 5° C. Then 0.14 mmol DIC were added and themixture is stirred for 20 min at 15° C. and added then to 0.1 mmol of aresin-bound C-terminal fragment and stirred for additional 6 h at RT.The completion of the condensation reaction is checked by the Kaisertest. In the cases where the Kaiser test remained blue a secondcondensation was performed in order to drive the condensation intocompletion.

Example 12 Synthesis of Partially Protected Peptides by the Condensationof an N-Terminal Protected Fragment with a C-Terminal Protected Fragmentin Solution

General Procedure

To a solution of 0.15 mmol/ml of an N-terminal protected fragment in DCMare added 0.2 mmol HOBt and the resulting solution is cooled to 5° C.Then 0.15 mmol EDAC were added and the mixture is stirred for 20 min at15° C. and added then to 0.15 mmol of a C-terminal protected fragmentand stirred for additional 2-5 h at RT. The completion of thecondensation reaction is checked by HPLC. In the cases where anincomplete condensation was observed an additional portion of 0.015 mmolEDAC was added and the reaction was left to proceed for an additionalhour at RT.

Example 13 Deprotection and Simultaneous Cleavage from the Resin ofPeptides

General Method

1.00 g of the protected resin-bound peptide, produced as described aboveis treated with 20 mL TFA/DTT/water (90:5:5) for 3 h at 5° C. and for 1h at 15° C. The resin is then washed 3× with the cleavage solution andthe combined filtrates are then concentrated in vacuum and crude peptideis precipitated by the addition of ether, washed several times withether and dried in vacuum until constant weight over KOH.

Example 14 Peptide Deprotection

General Method

1.00 g of the protected peptide, produced as described above was treatedwith 20 mL TFA/DTT/water (90:5:5) for 3 h at 5° C. and for 1 h at 15° C.The resulting solution is concentrated in vacuum and then thedeprotected peptide was precipitated by the addition of diisopropyletherand washed three times with 10 mL diisopropylether. The resulting solidwas dried in vacuum (25° C., 15 Torr) until constant weight under KOH.

Example 15 Purification of Crude Peptides Isolation of Peptides

General Procedure

The solution of the peptides obtained as described above wasconcentrated in vacuum and ice water and ether were added. Afterseparation of the organic layer the remaining water solution of thepeptide was extracted for additional two times with ether and theresulting solution was sparged with nitrogen or helium, filtered anddirectly loaded on a semipreparative column 10×25 cm, Lichrospher 100,RP-18, 12 micron (Merck); Phase A=1%-TFA in acetonitrile, phase B=1%-TFAin water; or Kromasil. HPLC fractions containing the purified peptidewere concentrated in vacuum to remove as much as possible the containedacetonitrile and lyophilized using a standard lyophilisation program.

Examples 16 to 23, as noted below, were performed using the aboveprocedures to prepare the listed compounds.

Example 16

Lanreotide

Example 17

Insulin B-chain

Example 18

Salmon Calcitonin

Example 19

Octreotide

Example 20

Exenatide

Example 21

Pramlintide

Example 22

Tetracosactide (ACTH 1-24)

Example 23

Bivalirudin

What is claimed is:
 1. A resin conjugate of the formula I or II,wherein:

Hya is the residue of a hydroxy amino acid; Pr¹ is H, or an aminoprotecting group which is orthogonal to the resin and to otherprotecting groups; A is a hydroxyl group or a hydroxyl group protectedby an acid sensitive hydroxyl protecting group selected from the groupconsisting of tBu, Trt and Clt; X, Y, Z and V are each independently asubstituent on the ortho, meta or para positions and is selected fromselected from the group consisting of H, Cl, F, C₁₋₁₀ alkyl and C₁₋₁₀alkoxy; and P is an insoluble solid support or an insoluble linker-resinconjugate suitable for the solid phase synthesis of peptides or a resinconjugate of the formula wherein:

Pr¹ is H or an amino protecting group, which is orthogonal to the resinand to other protecting groups; Pr² is H or a hydroxyl protecting groupwhich is orthogonal to the resin; R³ and R⁴ are each independently H orC₁₋₁₀ alkyl; X, Y, Z and V are each independently on the ortho, meta orpara positions selected from the group consisting of H, Cl, F, C₁₋₁₀alkyl and C₁₋₁₀ alkoxy; and P is an insoluble solid support or aninsoluble linker-resin conjugate suitable for the solid phase synthesisof peptides.
 2. A method for the preparation of the resin conjugate ofthe formulae I-VI of claim 1 comprising the following steps: preparing ahydroxyl containing amino acid or amino alcohol or peptide derivativethat is unprotected on at least one of the side chains of the containedhydroxyl amino acids or of the contained amino alcohol or selectivelydeprotecting the hydroxyl amino acid or the hydroxyl amino alcohol or apeptide derivative at the side chain of the hydroxyl amino acid or thehydroxyl amino alcohol and then attaching it to a suitable resin by itsreaction with a resin halide, wherein the resin is selected from thegroup of the trityl type resins and linkers or the benzhydryl typeresins or the benzyl-type resins; and an alcohol or thioalcohol is addedto mask any unreacted resin halide, to form the resin conjugate of theformulae I-VI.
 3. A process for the solid phase synthesis ofbiologically active free or partially protected peptides, cyclicpeptides and peptaibols, wherein the process comprises the use of theresin conjugates of claim 1 as functionalized resins in the solid phasepeptide synthesis.
 4. A partially protected peptide of the formula:

wherein: A is H or an amino protecting group selected from Fmoc, Boc,Trt, Nps, Mtt or Mmt; D- designates the chirality of the amino acid thatfollows as a D-amino acid; B is a thiol protecting group selected fromthe group consisting of Trt, Mmt, Acm and StBu; C is H or Boc; E is ahydroxy protecting group selected from the group consisting of Clt, Trtand tBu; and Resin is H or an acid labile resin suitable for solid-phasepeptide synthesis.
 5. The peptide of claim 4, wherein the peptide is aresin bound octreotide.
 6. A process for preparing octreotide, theprocess comprising: treating the peptide resin conjugate of claim 5 witha mild acid to obtain a peptide; and oxidizing the obtained peptidesolution using a suitable oxidizing agent selected from air, hydrogenperoxide, DMSO or iodine, to form octreotide.
 7. A process for preparingoctreotide, the process comprising: treating the peptide resin conjugateof claim 5 with a mild acid to obtain a peptide; deprotecting, purifyingand lyophilizing the peptide, to form octreotide, wherein the octreotidehas a purity of >99%.
 8. A resin conjugate of the formula III-VI,wherein:

Pr¹ is H or an amino protecting group, which is orthogonal to the resinand to other protecting groups; Pr² is H or a hydroxyl protecting groupwhich is orthogonal to the resin; R³ and R⁴ are each independently H orC₁₋₁₀ alkyl; X, Y, Z and V are each independently on the ortho, meta orpara positions selected from the group consisting of H, Cl, F, C₁₋₁₀alkyl and C₁₋₁₀ alkoxy; and P is an insoluble solid support or aninsoluble linker-resin conjugate suitable for the solid phase synthesisof peptides.
 9. The process of claim 6, wherein the mild acid comprisesa solution of trifluoroacetic acid optionally containing scavengers. 10.The process of claim 7, wherein the mild acid comprises a solution oftrifluoroacetic acid containing iodine.